FDA UDI In Commercial Distribution 🇺🇸 United States

Swabeze

DI: 10817522013343 · Model: KMI-LA · KENTEC MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Swabeze
Primary DI
10817522013343
Version / Model
KMI-LA
Catalog Number
KMI-LA
Company Name
KENTEC MEDICAL, INC.
Labeler DUNS
066175613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-20
Public Version
1
Public Version Date
2024-06-28
Public Version Status
New
Public Device Record Key
0ee0cf00-b68b-49a5-86a4-e31a9c2a1687

Device Description

low absorption foam swab

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXF Applicator, Absorbent Tipped, Non-Sterile

GMDN Terms

Code Name
33722 General-purpose absorbent tip applicator/swab, single-use

Identifiers

Type ID
Package 20817522013340
Primary 10817522013343
Package 30817522013347